Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - femtos GmbH

Address:

Universitaetsstrasse 136

Bochum

44799

Germany

Authorised Representative/ UK Responsible Person
Name: phenox UK Ltd
Address:

Phenox UK Ltd 23 Greenbox

Westonhall Road Stoke Prior

Bromsgrove

B60 4AL

England United Kingdom

Code/Term Type

Thrombectomy wire-net Thrombectomy wire-net Class III

Bare-metal intracranial vascular stent Bare-metal intracranial vascular stent Class III

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
Thrombectomy wire-net	Thrombectomy wire-net	Class III
Bare-metal intracranial vascular stent	Bare-metal intracranial vascular stent	Class III